Taiwan FDA registration 6ea720d6d7611d7162ef76034335d3ee
"Stryker" non-powered therapeutic mattress (unsterilized)
TW: "史賽克" 非動力式治療床墊 (未滅菌)
Taiwan·Risk Class 1·STRYKER MEDICAL·Registered Jan 16, 2006 – Jan 16, 2026CancelledRegistration details
- Analysis ID
- 6ea720d6d7611d7162ef76034335d3ee
- Customs Code
- DHA04400252401
Company information
- Manufacturer
- STRYKER MEDICAL
- Manufacturer Country
- United States
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- Intended Use
- Has the function of supporting the patient to prevent excessive stress on the part of the body. This device can be used to treat or avoid bedsores caused by bed rest.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5150 Non-powered floating therapy mattress
- Import Information
- import
Dates and status
- Registration Date
- Jan 16, 2006
- Expiry Date
- Jan 16, 2026
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "Stryker" non-powered therapeutic mattress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6ea720d6d7611d7162ef76034335d3ee and manufactured by STRYKER MEDICAL. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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